A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13933429



Internal ID3935245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110249625..110251551hg38UCSC Ensembl
Innerchr10:110249679..110251498hg38UCSC Ensembl
Outerchr10:110249572..110251605hg38UCSC Ensembl
chr10:112009383..112011309hg19UCSC Ensembl
Innerchr10:112009437..112011256hg19UCSC Ensembl
Outerchr10:112009330..112011363hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg381927
hg191927
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624536
Supporting Variants
SamplesNA18940
Known GenesMXI1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13933429
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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